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Advances and Perspectives in Genetics of Congenital Thyroid Disorders Associated with Thyroglobulin Gene Mutations

<p>Dyshormonogenesis due to thyroglobulin (TG) gene mutations is a rare cause of congenital hypothyroidism with an estimated incidence of approximately 1 in 100,000 newborns. The TG gene is organized in 48 exons, spanning over 270 kb on human chromosome 8q24. The human TG mRNA is 8.5 Kb long a...

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主要な著者:	Héctor M.Targovnik (著者), Cintia E.Citterio (著者), Sofi a Siffo (著者), Carina M.Rivolta (著者)
フォーマット:	図書
出版事項:	Open Journal of Biological Sciences - Peertechz Publications, 2016-12-19.
主題:	Review Article
オンライン･アクセス:	Connect to this object online.
タグ:	タグ追加タグなし, このレコードへの初めてのタグを付けませんか!

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